Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 0 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 5 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0030119 | AP-type membrane coat adaptor complex | 3 | 12 |
GO:0030121 | AP-1 adaptor complex | 5 | 12 |
GO:0030131 | clathrin adaptor complex | 4 | 12 |
GO:0032991 | protein-containing complex | 1 | 12 |
GO:0098796 | membrane protein complex | 2 | 12 |
Related structures:
AlphaFold database: Q4Q2E4
Term | Name | Level | Count |
---|---|---|---|
GO:0006810 | transport | 3 | 12 |
GO:0006886 | intracellular protein transport | 4 | 12 |
GO:0006892 | post-Golgi vesicle-mediated transport | 6 | 2 |
GO:0006896 | Golgi to vacuole transport | 5 | 2 |
GO:0006897 | endocytosis | 5 | 2 |
GO:0006898 | receptor-mediated endocytosis | 6 | 2 |
GO:0007034 | vacuolar transport | 4 | 2 |
GO:0008104 | protein localization | 4 | 12 |
GO:0009987 | cellular process | 1 | 12 |
GO:0015031 | protein transport | 4 | 12 |
GO:0016192 | vesicle-mediated transport | 4 | 12 |
GO:0033036 | macromolecule localization | 2 | 12 |
GO:0045184 | establishment of protein localization | 3 | 12 |
GO:0046907 | intracellular transport | 3 | 12 |
GO:0048193 | Golgi vesicle transport | 5 | 2 |
GO:0051179 | localization | 1 | 12 |
GO:0051234 | establishment of localization | 2 | 12 |
GO:0051641 | cellular localization | 2 | 12 |
GO:0051649 | establishment of localization in cell | 3 | 12 |
GO:0070727 | cellular macromolecule localization | 3 | 12 |
GO:0071702 | organic substance transport | 4 | 12 |
GO:0071705 | nitrogen compound transport | 4 | 12 |
Term | Name | Level | Count |
---|---|---|---|
GO:0005488 | binding | 1 | 2 |
GO:0005515 | protein binding | 2 | 2 |
GO:0030276 | clathrin binding | 3 | 2 |
GO:0030674 | protein-macromolecule adaptor activity | 2 | 2 |
GO:0035615 | clathrin adaptor activity | 4 | 2 |
GO:0060090 | molecular adaptor activity | 1 | 2 |
GO:0140312 | cargo adaptor activity | 3 | 2 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 148 | 152 | PF00656 | 0.443 |
CLV_C14_Caspase3-7 | 2 | 6 | PF00656 | 0.609 |
CLV_C14_Caspase3-7 | 288 | 292 | PF00656 | 0.308 |
CLV_C14_Caspase3-7 | 331 | 335 | PF00656 | 0.326 |
CLV_C14_Caspase3-7 | 655 | 659 | PF00656 | 0.490 |
CLV_NRD_NRD_1 | 119 | 121 | PF00675 | 0.377 |
CLV_NRD_NRD_1 | 176 | 178 | PF00675 | 0.428 |
CLV_NRD_NRD_1 | 224 | 226 | PF00675 | 0.430 |
CLV_NRD_NRD_1 | 349 | 351 | PF00675 | 0.221 |
CLV_NRD_NRD_1 | 36 | 38 | PF00675 | 0.469 |
CLV_NRD_NRD_1 | 376 | 378 | PF00675 | 0.295 |
CLV_NRD_NRD_1 | 487 | 489 | PF00675 | 0.323 |
CLV_PCSK_KEX2_1 | 119 | 121 | PF00082 | 0.440 |
CLV_PCSK_KEX2_1 | 375 | 377 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 147 | 151 | PF00082 | 0.308 |
CLV_PCSK_SKI1_1 | 167 | 171 | PF00082 | 0.124 |
CLV_PCSK_SKI1_1 | 226 | 230 | PF00082 | 0.314 |
CLV_PCSK_SKI1_1 | 233 | 237 | PF00082 | 0.304 |
CLV_PCSK_SKI1_1 | 376 | 380 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 437 | 441 | PF00082 | 0.333 |
CLV_PCSK_SKI1_1 | 452 | 456 | PF00082 | 0.299 |
CLV_PCSK_SKI1_1 | 488 | 492 | PF00082 | 0.324 |
CLV_PCSK_SKI1_1 | 50 | 54 | PF00082 | 0.318 |
CLV_PCSK_SKI1_1 | 511 | 515 | PF00082 | 0.349 |
CLV_PCSK_SKI1_1 | 544 | 548 | PF00082 | 0.381 |
DEG_APCC_DBOX_1 | 146 | 154 | PF00400 | 0.323 |
DEG_APCC_DBOX_1 | 451 | 459 | PF00400 | 0.338 |
DEG_APCC_DBOX_1 | 49 | 57 | PF00400 | 0.323 |
DEG_ODPH_VHL_1 | 763 | 775 | PF01847 | 0.377 |
DOC_CYCLIN_RxL_1 | 233 | 242 | PF00134 | 0.308 |
DOC_CYCLIN_RxL_1 | 374 | 384 | PF00134 | 0.342 |
DOC_CYCLIN_RxL_1 | 449 | 459 | PF00134 | 0.260 |
DOC_CYCLIN_yClb1_LxF_4 | 334 | 340 | PF00134 | 0.365 |
DOC_MAPK_gen_1 | 165 | 172 | PF00069 | 0.182 |
DOC_MAPK_gen_1 | 375 | 383 | PF00069 | 0.294 |
DOC_MAPK_gen_1 | 440 | 450 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 48 | 56 | PF00069 | 0.323 |
DOC_MAPK_gen_1 | 488 | 496 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 375 | 383 | PF00069 | 0.308 |
DOC_MAPK_MEF2A_6 | 488 | 496 | PF00069 | 0.428 |
DOC_MAPK_MEF2A_6 | 50 | 58 | PF00069 | 0.427 |
DOC_MAPK_MEF2A_6 | 785 | 793 | PF00069 | 0.305 |
DOC_MAPK_MEF2A_6 | 85 | 93 | PF00069 | 0.311 |
DOC_MAPK_NFAT4_5 | 376 | 384 | PF00069 | 0.323 |
DOC_MAPK_RevD_3 | 362 | 376 | PF00069 | 0.365 |
DOC_PP1_RVXF_1 | 258 | 265 | PF00149 | 0.308 |
DOC_PP2B_LxvP_1 | 393 | 396 | PF13499 | 0.323 |
DOC_PP2B_PxIxI_1 | 44 | 50 | PF00149 | 0.455 |
DOC_USP7_MATH_1 | 310 | 314 | PF00917 | 0.342 |
DOC_USP7_MATH_1 | 400 | 404 | PF00917 | 0.441 |
DOC_USP7_MATH_1 | 668 | 672 | PF00917 | 0.704 |
DOC_USP7_MATH_1 | 675 | 679 | PF00917 | 0.701 |
DOC_USP7_MATH_1 | 684 | 688 | PF00917 | 0.674 |
DOC_USP7_MATH_1 | 705 | 709 | PF00917 | 0.498 |
DOC_USP7_MATH_1 | 758 | 762 | PF00917 | 0.360 |
DOC_USP7_MATH_2 | 608 | 614 | PF00917 | 0.641 |
DOC_USP7_UBL2_3 | 544 | 548 | PF12436 | 0.393 |
DOC_WW_Pin1_4 | 157 | 162 | PF00397 | 0.428 |
DOC_WW_Pin1_4 | 691 | 696 | PF00397 | 0.761 |
LIG_14-3-3_CanoR_1 | 119 | 125 | PF00244 | 0.416 |
LIG_14-3-3_CanoR_1 | 225 | 235 | PF00244 | 0.301 |
LIG_14-3-3_CanoR_1 | 243 | 249 | PF00244 | 0.311 |
LIG_14-3-3_CanoR_1 | 327 | 333 | PF00244 | 0.365 |
LIG_14-3-3_CanoR_1 | 415 | 421 | PF00244 | 0.421 |
LIG_14-3-3_CanoR_1 | 750 | 755 | PF00244 | 0.424 |
LIG_14-3-3_CanoR_1 | 790 | 796 | PF00244 | 0.374 |
LIG_Actin_WH2_2 | 142 | 160 | PF00022 | 0.221 |
LIG_Actin_WH2_2 | 322 | 340 | PF00022 | 0.365 |
LIG_Actin_WH2_2 | 425 | 442 | PF00022 | 0.455 |
LIG_AP2alpha_2 | 254 | 256 | PF02296 | 0.323 |
LIG_BIR_II_1 | 1 | 5 | PF00653 | 0.568 |
LIG_BIR_III_2 | 42 | 46 | PF00653 | 0.416 |
LIG_BIR_III_2 | 551 | 555 | PF00653 | 0.416 |
LIG_BRCT_BRCA1_1 | 434 | 438 | PF00533 | 0.454 |
LIG_BRCT_BRCA1_1 | 477 | 481 | PF00533 | 0.342 |
LIG_BRCT_BRCA1_1 | 658 | 662 | PF00533 | 0.657 |
LIG_BRCT_BRCA1_1 | 722 | 726 | PF00533 | 0.441 |
LIG_BRCT_BRCA1_2 | 434 | 440 | PF00533 | 0.455 |
LIG_Clathr_ClatBox_1 | 630 | 634 | PF01394 | 0.650 |
LIG_deltaCOP1_diTrp_1 | 471 | 481 | PF00928 | 0.455 |
LIG_DLG_GKlike_1 | 120 | 127 | PF00625 | 0.377 |
LIG_eIF4E_1 | 124 | 130 | PF01652 | 0.428 |
LIG_eIF4E_1 | 537 | 543 | PF01652 | 0.308 |
LIG_eIF4E_1 | 88 | 94 | PF01652 | 0.428 |
LIG_FHA_1 | 10 | 16 | PF00498 | 0.460 |
LIG_FHA_1 | 196 | 202 | PF00498 | 0.386 |
LIG_FHA_1 | 204 | 210 | PF00498 | 0.403 |
LIG_FHA_1 | 227 | 233 | PF00498 | 0.316 |
LIG_FHA_1 | 291 | 297 | PF00498 | 0.365 |
LIG_FHA_1 | 317 | 323 | PF00498 | 0.365 |
LIG_FHA_1 | 380 | 386 | PF00498 | 0.301 |
LIG_FHA_1 | 460 | 466 | PF00498 | 0.393 |
LIG_FHA_1 | 577 | 583 | PF00498 | 0.319 |
LIG_FHA_1 | 622 | 628 | PF00498 | 0.640 |
LIG_FHA_1 | 644 | 650 | PF00498 | 0.713 |
LIG_FHA_1 | 751 | 757 | PF00498 | 0.322 |
LIG_FHA_2 | 101 | 107 | PF00498 | 0.308 |
LIG_FHA_2 | 19 | 25 | PF00498 | 0.411 |
LIG_FHA_2 | 243 | 249 | PF00498 | 0.308 |
LIG_FHA_2 | 286 | 292 | PF00498 | 0.330 |
LIG_FHA_2 | 512 | 518 | PF00498 | 0.455 |
LIG_FHA_2 | 563 | 569 | PF00498 | 0.333 |
LIG_FHA_2 | 624 | 630 | PF00498 | 0.641 |
LIG_FXI_DFP_1 | 582 | 586 | PF00024 | 0.516 |
LIG_LIR_Gen_1 | 123 | 132 | PF02991 | 0.427 |
LIG_LIR_Gen_1 | 253 | 264 | PF02991 | 0.285 |
LIG_LIR_Gen_1 | 352 | 361 | PF02991 | 0.398 |
LIG_LIR_Gen_1 | 435 | 446 | PF02991 | 0.461 |
LIG_LIR_Gen_1 | 501 | 510 | PF02991 | 0.333 |
LIG_LIR_Gen_1 | 529 | 539 | PF02991 | 0.342 |
LIG_LIR_Gen_1 | 577 | 586 | PF02991 | 0.308 |
LIG_LIR_Gen_1 | 592 | 601 | PF02991 | 0.463 |
LIG_LIR_Gen_1 | 65 | 75 | PF02991 | 0.455 |
LIG_LIR_Gen_1 | 711 | 720 | PF02991 | 0.399 |
LIG_LIR_Gen_1 | 723 | 731 | PF02991 | 0.443 |
LIG_LIR_LC3C_4 | 728 | 731 | PF02991 | 0.338 |
LIG_LIR_Nem_3 | 123 | 127 | PF02991 | 0.427 |
LIG_LIR_Nem_3 | 253 | 259 | PF02991 | 0.285 |
LIG_LIR_Nem_3 | 352 | 356 | PF02991 | 0.398 |
LIG_LIR_Nem_3 | 435 | 441 | PF02991 | 0.461 |
LIG_LIR_Nem_3 | 501 | 505 | PF02991 | 0.333 |
LIG_LIR_Nem_3 | 529 | 534 | PF02991 | 0.323 |
LIG_LIR_Nem_3 | 577 | 581 | PF02991 | 0.362 |
LIG_LIR_Nem_3 | 664 | 670 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 711 | 715 | PF02991 | 0.409 |
LIG_LIR_Nem_3 | 723 | 729 | PF02991 | 0.426 |
LIG_LIR_Nem_3 | 80 | 84 | PF02991 | 0.392 |
LIG_LYPXL_SIV_4 | 45 | 53 | PF13949 | 0.428 |
LIG_LYPXL_SIV_4 | 765 | 773 | PF13949 | 0.416 |
LIG_MLH1_MIPbox_1 | 658 | 662 | PF16413 | 0.491 |
LIG_NRBOX | 341 | 347 | PF00104 | 0.308 |
LIG_PCNA_yPIPBox_3 | 258 | 266 | PF02747 | 0.308 |
LIG_PCNA_yPIPBox_3 | 280 | 294 | PF02747 | 0.320 |
LIG_PCNA_yPIPBox_3 | 535 | 543 | PF02747 | 0.393 |
LIG_Pex14_1 | 430 | 434 | PF04695 | 0.365 |
LIG_SH2_CRK | 401 | 405 | PF00017 | 0.401 |
LIG_SH2_CRK | 578 | 582 | PF00017 | 0.342 |
LIG_SH2_PTP2 | 46 | 49 | PF00017 | 0.455 |
LIG_SH2_PTP2 | 502 | 505 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 434 | 438 | PF00017 | 0.365 |
LIG_SH2_STAP1 | 578 | 582 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 185 | 188 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 189 | 192 | PF00017 | 0.428 |
LIG_SH2_STAT5 | 46 | 49 | PF00017 | 0.359 |
LIG_SH2_STAT5 | 502 | 505 | PF00017 | 0.365 |
LIG_SH2_STAT5 | 57 | 60 | PF00017 | 0.248 |
LIG_SH2_STAT5 | 578 | 581 | PF00017 | 0.319 |
LIG_SH2_STAT5 | 795 | 798 | PF00017 | 0.320 |
LIG_SH2_STAT5 | 88 | 91 | PF00017 | 0.308 |
LIG_SH3_3 | 580 | 586 | PF00018 | 0.541 |
LIG_SH3_3 | 595 | 601 | PF00018 | 0.603 |
LIG_SH3_3 | 636 | 642 | PF00018 | 0.710 |
LIG_SUMO_SIM_anti_2 | 382 | 387 | PF11976 | 0.308 |
LIG_SUMO_SIM_anti_2 | 501 | 507 | PF11976 | 0.365 |
LIG_SUMO_SIM_anti_2 | 745 | 750 | PF11976 | 0.454 |
LIG_SUMO_SIM_anti_2 | 96 | 106 | PF11976 | 0.439 |
LIG_SUMO_SIM_par_1 | 205 | 210 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 318 | 324 | PF11976 | 0.455 |
LIG_SUMO_SIM_par_1 | 380 | 387 | PF11976 | 0.342 |
LIG_SUMO_SIM_par_1 | 453 | 460 | PF11976 | 0.349 |
LIG_SUMO_SIM_par_1 | 579 | 584 | PF11976 | 0.467 |
LIG_SUMO_SIM_par_1 | 607 | 613 | PF11976 | 0.693 |
LIG_SUMO_SIM_par_1 | 96 | 106 | PF11976 | 0.319 |
LIG_TRAF2_1 | 21 | 24 | PF00917 | 0.423 |
LIG_TYR_ITIM | 122 | 127 | PF00017 | 0.416 |
LIG_TYR_ITIM | 300 | 305 | PF00017 | 0.308 |
LIG_TYR_ITIM | 399 | 404 | PF00017 | 0.317 |
LIG_TYR_ITIM | 86 | 91 | PF00017 | 0.323 |
LIG_UBA3_1 | 149 | 158 | PF00899 | 0.416 |
LIG_UBA3_1 | 454 | 463 | PF00899 | 0.420 |
LIG_UBA3_1 | 725 | 734 | PF00899 | 0.377 |
LIG_WRC_WIRS_1 | 557 | 562 | PF05994 | 0.423 |
LIG_WRC_WIRS_1 | 590 | 595 | PF05994 | 0.497 |
MOD_CK1_1 | 242 | 248 | PF00069 | 0.308 |
MOD_CK1_1 | 250 | 256 | PF00069 | 0.308 |
MOD_CK1_1 | 272 | 278 | PF00069 | 0.342 |
MOD_CK1_1 | 3 | 9 | PF00069 | 0.536 |
MOD_CK1_1 | 403 | 409 | PF00069 | 0.377 |
MOD_CK1_1 | 459 | 465 | PF00069 | 0.344 |
MOD_CK1_1 | 523 | 529 | PF00069 | 0.385 |
MOD_CK1_1 | 562 | 568 | PF00069 | 0.356 |
MOD_CK1_1 | 643 | 649 | PF00069 | 0.719 |
MOD_CK1_1 | 678 | 684 | PF00069 | 0.661 |
MOD_CK1_1 | 687 | 693 | PF00069 | 0.761 |
MOD_CK1_1 | 733 | 739 | PF00069 | 0.390 |
MOD_CK2_1 | 100 | 106 | PF00069 | 0.308 |
MOD_CK2_1 | 18 | 24 | PF00069 | 0.421 |
MOD_CK2_1 | 416 | 422 | PF00069 | 0.377 |
MOD_GlcNHglycan | 215 | 218 | PF01048 | 0.382 |
MOD_GlcNHglycan | 229 | 232 | PF01048 | 0.409 |
MOD_GlcNHglycan | 246 | 252 | PF01048 | 0.453 |
MOD_GlcNHglycan | 32 | 35 | PF01048 | 0.393 |
MOD_GlcNHglycan | 664 | 667 | PF01048 | 0.659 |
MOD_GlcNHglycan | 677 | 680 | PF01048 | 0.685 |
MOD_GlcNHglycan | 689 | 692 | PF01048 | 0.697 |
MOD_GlcNHglycan | 716 | 719 | PF01048 | 0.337 |
MOD_GlcNHglycan | 80 | 84 | PF01048 | 0.428 |
MOD_GSK3_1 | 111 | 118 | PF00069 | 0.428 |
MOD_GSK3_1 | 238 | 245 | PF00069 | 0.316 |
MOD_GSK3_1 | 269 | 276 | PF00069 | 0.311 |
MOD_GSK3_1 | 323 | 330 | PF00069 | 0.365 |
MOD_GSK3_1 | 416 | 423 | PF00069 | 0.396 |
MOD_GSK3_1 | 517 | 524 | PF00069 | 0.398 |
MOD_GSK3_1 | 559 | 566 | PF00069 | 0.392 |
MOD_GSK3_1 | 640 | 647 | PF00069 | 0.692 |
MOD_GSK3_1 | 652 | 659 | PF00069 | 0.525 |
MOD_GSK3_1 | 662 | 669 | PF00069 | 0.557 |
MOD_GSK3_1 | 687 | 694 | PF00069 | 0.742 |
MOD_N-GLC_1 | 529 | 534 | PF02516 | 0.374 |
MOD_N-GLC_1 | 562 | 567 | PF02516 | 0.369 |
MOD_NEK2_1 | 149 | 154 | PF00069 | 0.361 |
MOD_NEK2_1 | 238 | 243 | PF00069 | 0.295 |
MOD_NEK2_1 | 328 | 333 | PF00069 | 0.373 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.249 |
MOD_NEK2_1 | 379 | 384 | PF00069 | 0.323 |
MOD_NEK2_1 | 591 | 596 | PF00069 | 0.532 |
MOD_NEK2_1 | 650 | 655 | PF00069 | 0.652 |
MOD_NEK2_1 | 720 | 725 | PF00069 | 0.355 |
MOD_NEK2_1 | 742 | 747 | PF00069 | 0.410 |
MOD_NEK2_1 | 806 | 811 | PF00069 | 0.456 |
MOD_NEK2_1 | 9 | 14 | PF00069 | 0.520 |
MOD_NEK2_2 | 684 | 689 | PF00069 | 0.768 |
MOD_PIKK_1 | 457 | 463 | PF00454 | 0.403 |
MOD_PIKK_1 | 591 | 597 | PF00454 | 0.591 |
MOD_PIKK_1 | 612 | 618 | PF00454 | 0.657 |
MOD_PIKK_1 | 652 | 658 | PF00454 | 0.748 |
MOD_PIKK_1 | 668 | 674 | PF00454 | 0.716 |
MOD_PIKK_1 | 74 | 80 | PF00454 | 0.428 |
MOD_PIKK_1 | 775 | 781 | PF00454 | 0.441 |
MOD_PIKK_1 | 806 | 812 | PF00454 | 0.347 |
MOD_PKA_2 | 242 | 248 | PF00069 | 0.323 |
MOD_PKA_2 | 367 | 373 | PF00069 | 0.299 |
MOD_PKA_2 | 791 | 797 | PF00069 | 0.455 |
MOD_Plk_1 | 370 | 376 | PF00069 | 0.308 |
MOD_Plk_1 | 379 | 385 | PF00069 | 0.308 |
MOD_Plk_1 | 432 | 438 | PF00069 | 0.308 |
MOD_Plk_1 | 475 | 481 | PF00069 | 0.297 |
MOD_Plk_1 | 529 | 535 | PF00069 | 0.393 |
MOD_Plk_1 | 562 | 568 | PF00069 | 0.410 |
MOD_Plk_1 | 576 | 582 | PF00069 | 0.224 |
MOD_Plk_1 | 644 | 650 | PF00069 | 0.737 |
MOD_Plk_1 | 684 | 690 | PF00069 | 0.743 |
MOD_Plk_2-3 | 100 | 106 | PF00069 | 0.308 |
MOD_Plk_4 | 100 | 106 | PF00069 | 0.449 |
MOD_Plk_4 | 149 | 155 | PF00069 | 0.398 |
MOD_Plk_4 | 197 | 203 | PF00069 | 0.344 |
MOD_Plk_4 | 341 | 347 | PF00069 | 0.322 |
MOD_Plk_4 | 381 | 387 | PF00069 | 0.406 |
MOD_Plk_4 | 416 | 422 | PF00069 | 0.377 |
MOD_Plk_4 | 577 | 583 | PF00069 | 0.308 |
MOD_Plk_4 | 645 | 651 | PF00069 | 0.775 |
MOD_Plk_4 | 656 | 662 | PF00069 | 0.705 |
MOD_Plk_4 | 678 | 684 | PF00069 | 0.661 |
MOD_Plk_4 | 720 | 726 | PF00069 | 0.418 |
MOD_ProDKin_1 | 157 | 163 | PF00069 | 0.428 |
MOD_ProDKin_1 | 691 | 697 | PF00069 | 0.760 |
TRG_DiLeu_BaEn_1 | 100 | 105 | PF01217 | 0.443 |
TRG_DiLeu_BaEn_1 | 125 | 130 | PF01217 | 0.428 |
TRG_DiLeu_BaEn_1 | 501 | 506 | PF01217 | 0.323 |
TRG_DiLeu_BaEn_1 | 577 | 582 | PF01217 | 0.365 |
TRG_DiLeu_BaEn_1 | 71 | 76 | PF01217 | 0.308 |
TRG_DiLeu_BaLyEn_6 | 11 | 16 | PF01217 | 0.539 |
TRG_DiLeu_BaLyEn_6 | 389 | 394 | PF01217 | 0.316 |
TRG_ENDOCYTIC_2 | 124 | 127 | PF00928 | 0.428 |
TRG_ENDOCYTIC_2 | 302 | 305 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 401 | 404 | PF00928 | 0.311 |
TRG_ENDOCYTIC_2 | 46 | 49 | PF00928 | 0.359 |
TRG_ENDOCYTIC_2 | 502 | 505 | PF00928 | 0.323 |
TRG_ENDOCYTIC_2 | 51 | 54 | PF00928 | 0.313 |
TRG_ENDOCYTIC_2 | 57 | 60 | PF00928 | 0.248 |
TRG_ENDOCYTIC_2 | 578 | 581 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 88 | 91 | PF00928 | 0.308 |
TRG_ER_diArg_1 | 374 | 377 | PF00400 | 0.308 |
TRG_ER_diArg_1 | 47 | 50 | PF00400 | 0.323 |
TRG_ER_diArg_1 | 789 | 792 | PF00400 | 0.455 |
TRG_NES_CRM1_1 | 199 | 210 | PF08389 | 0.423 |
TRG_NES_CRM1_1 | 740 | 755 | PF08389 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 14 | 18 | PF00026 | 0.568 |
TRG_Pf-PMV_PEXEL_1 | 147 | 151 | PF00026 | 0.428 |
TRG_Pf-PMV_PEXEL_1 | 392 | 397 | PF00026 | 0.308 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N0P707 | Leptomonas seymouri | 71% | 98% |
A0A0N1I3J7 | Leptomonas seymouri | 20% | 74% |
A0A0N1PA13 | Leptomonas seymouri | 26% | 84% |
A0A0S4JAH1 | Bodo saltans | 25% | 77% |
A0A0S4JIE7 | Bodo saltans | 41% | 93% |
A0A1X0NLY4 | Trypanosomatidae | 25% | 84% |
A0A1X0P1U8 | Trypanosomatidae | 25% | 79% |
A0A1X0PA59 | Trypanosomatidae | 51% | 100% |
A0A3Q8IHK1 | Leishmania donovani | 93% | 98% |
A0A3S7WPR4 | Leishmania donovani | 26% | 84% |
A0A422NSY3 | Trypanosoma rangeli | 49% | 100% |
A0A422NT90 | Trypanosoma rangeli | 25% | 84% |
A0A422P3I9 | Trypanosoma rangeli | 25% | 81% |
A4H4U8 | Leishmania braziliensis | 26% | 85% |
A4HBC0 | Leishmania braziliensis | 82% | 97% |
A4HT27 | Leishmania infantum | 26% | 84% |
A4IAG8 | Leishmania infantum | 93% | 98% |
C9ZLS4 | Trypanosoma brucei gambiense (strain MHOM/CI/86/DAL972) | 47% | 100% |
E9AL15 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 26% | 84% |
E9B5J2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 89% | 98% |
O43747 | Homo sapiens | 30% | 99% |
O75843 | Homo sapiens | 35% | 100% |
O88512 | Mus musculus | 36% | 100% |
O94973 | Homo sapiens | 24% | 86% |
O95782 | Homo sapiens | 25% | 83% |
P17426 | Mus musculus | 25% | 83% |
P17427 | Mus musculus | 23% | 87% |
P18484 | Rattus norvegicus | 23% | 87% |
P22892 | Mus musculus | 30% | 99% |
P38065 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 22% | 79% |
P91926 | Drosophila melanogaster | 25% | 86% |
Q0VCK5 | Bos taurus | 24% | 87% |
Q12028 | Saccharomyces cerevisiae (strain ATCC 204508 / S288c) | 26% | 98% |
Q29N38 | Drosophila pseudoobscura pseudoobscura | 24% | 86% |
Q4QIT9 | Leishmania major | 26% | 84% |
Q5R5M2 | Pongo abelii | 30% | 99% |
Q7QG73 | Anopheles gambiae | 25% | 87% |
Q84K16 | Arabidopsis thaliana | 35% | 93% |
Q86KI1 | Dictyostelium discoideum | 29% | 82% |
Q8I8U2 | Dictyostelium discoideum | 38% | 91% |
Q8L7A9 | Arabidopsis thaliana | 27% | 87% |
Q8LPK4 | Arabidopsis thaliana | 26% | 80% |
Q8LPL6 | Arabidopsis thaliana | 26% | 80% |
Q99128 | Ustilago maydis (strain 521 / FGSC 9021) | 39% | 93% |
Q9C0W7 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 26% | 92% |
Q9UTL8 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 21% | 98% |
Q9UU81 | Schizosaccharomyces pombe (strain 972 / ATCC 24843) | 32% | 94% |
Q9ZUI6 | Arabidopsis thaliana | 33% | 94% |
V5B8U2 | Trypanosoma cruzi | 25% | 100% |
V5BW37 | Trypanosoma cruzi | 51% | 100% |